Nihon Kohden Corp.
Nihon Kohden Corp. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2015.
Top product codes for Nihon Kohden Corp.
Recent clearances by Nihon Kohden Corp.
- K130238 — NIHON KOHDEN AE-918P NEURO UNIT
- K122214 — TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)
- K120888 — PSG-1100 SLEEP DIAGNOSTIC SYSTEM
- K120397 — MEB-2300A NEUROPACK EVOKED POTENTIAL AND EMG MEASURING SYSTEM
- K110594 — GF-210R MULTI-GAS MODULE FOR NOHON KOHDEN BEDSIDE MONITORS
- K110410 — MS-120BK ELECTRIC STIMULATOR (EXTENSION UNIT)
- K110376 — PE-210AK SWITCH BOX
- K102106 — NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION
- K102376 — NIHON KOHDEN CNS-6200 SERIES CENTRAL NURSE STATION, MODEL CNS-6201
Data sourced from openFDA. This site is unofficial and independent of the FDA.